Clinical trial
A study of the effect of OC000459 on signs & symptoms in subjects with moderate to severe atopic dermatitis: A randomised double blind placebo controlled parallel group study
To assess the efficacy of OC000459 50 mg given once a day orally in comparison to placebo on the severity and extent of atopic dermatitis using the Eczema Area and Severity Index (EASI) over a 26 week period by subjects with active moderate to severe atopic dermatitis (AD) requiring treatment.
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Study start date | 2013-05-20 |